zoe Brunswick

The Brunswick's

Fundraising for Foundation for Prader-Willi Research UK
£1,082
raised of £2,000 target
by 62 supporters
Donations cannot currently be made to this page
Event: Tough Mudder Half North West 2017, from 9 September 2017 to 10 September 2017
We fund research in Prader-Willi Syndrome to give hope for a brighter future

Story

In August 2014, our friends Catherine and Jonathan welcomed their second baby boy into the world. William was diagnosed with Prader Willi Syndrome at birth. He spent his first 3 weeks in the Special Care Baby Unit at Wrexham Maelor Hospital and was fed through a Nasal Gastric tube in until he was 16 weeks.

Suffering from low muscle tone, Wills is a true fighter and only started to walk earlier this year. Not to let PWS get the better of him, he has just this month started nursery school #willpower!!

He is such a happy little boy who always has a smile on his face and loves being cuddled by his big brother James.

Prader-Willi syndrome (often called PWS) is a complex medical condition that affects both males and females throughout their lives. People with PWS may need extra support with health and development and in the areas of education and work.

Seeing the determination on Wills face to not let this define him has made us want to push ourselves physically to raise much needed funds for more research into Prader-Willi syndrome.

On Sunday 10th September, my husband Richard and I will be taking on the Tough Mudder Half at Cholmondely Castle. Not fully knowing what is going to face us on the day, this is going to take strength, determination and team work to tackle this enduring physical challenge. If a little boy like William can take his challenges in his stride then so can we #willpower!!!

Please sponsor us to support much needed research into this syndrome, helping us to contribute to an even brighter future for William and his family and all the other people who are affected by PWS.

Thanks for taking the time to visit our JustGiving page.

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About the charity

The mission of Foundation for Prader-Willi Research UK (FPWR UK) is to eliminate the challenges of Prader-Willi Syndrome through the advancement of research. High quality research will lead to more effective treatments and an eventual cure for this disorder. FPWR UK was founded in 2010 by parents of children with Prader-Willi Syndrome.

Donation summary

Total raised
£1,082.00
+ £213.00 Gift Aid
Online donations
£1,082.00
Offline donations
£0.00

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